Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2869546
CHRNA3
0.851 0.120 15 78615003 intron variant C/T snv 0.64 5
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 5
rs1133104
CLEC4A
1.000 0.120 12 8138526 3 prime UTR variant T/G snv 0.25 2
rs11727234 4 95886824 intergenic variant G/A snv 0.12 1
rs11877326 18 58836324 downstream gene variant A/C snv 0.32 1
rs17310107 7 25427204 intron variant A/G;T snv 1
rs2800342 9 30183555 intergenic variant T/A snv 0.91 1
rs34927688 8 8765284 intron variant C/G snv 0.15 1
rs35940501 2 17415423 intergenic variant C/T snv 0.10 1
rs56276612 5 40427283 intron variant G/T snv 0.18 1
rs57900878 14 33807301 downstream gene variant C/G snv 0.22 1
rs6583326 3 196590437 downstream gene variant T/C snv 0.65 1
rs7147984 14 43645922 intergenic variant T/C snv 0.11 1
rs1538101
BNC2
9 16710872 intron variant A/G snv 0.90 1
rs706042
BZW2
7 16696157 intron variant C/A;G;T snv 1
rs78226944
CRMP1
4 5855526 intron variant A/C snv 0.11 1
rs55684444
LILRA4
19 54336700 intron variant A/C;T snv 1
rs55946466
LINC00319
21 43451268 non coding transcript exon variant C/T snv 1
rs142735410
LINC01588 ; LINC01599
14 50016710 intron variant TTTTTTTTTTTT/-;T;TT;TTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT delins 1
rs56160206
LINC02731
11 134052045 intron variant A/-;AA;AAA delins 1
rs66549549
LOC101927404
18 64961187 intron variant G/A snv 0.19 1
rs9613645
LOC101929594 ; TTC28
22 28551414 intron variant A/T snv 5.3E-02 1
rs13335236
LOC105371064 ; PPL
16 4905255 intron variant T/C snv 8.5E-02 1
rs1445002
LOC105374736
5 40319775 intergenic variant C/A snv 0.15 1
rs72702916
NFIB
9 14485000 intergenic variant G/A;C;T snv 1